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Fig. 4. The cardiogenic mesoderm is required for liver specification.
(A) At the 32-cell stage, Xenopus embryos were injected with
Gsk3ß RNA (500 pg) into the D4 posterior endoderm cell. At stage 18,
endoderm explants were isolated from control and injected embryos, and
cultured with or without their associated mesoderm (orange) until stage 35
when they were assayed by RT-PCR. Foregut explants from uninjected embryos
were either left intact with the anterior endoderm and associated mesoderm
(AEM), or the anterior endoderm (AE, green) was separated from the mesoderm
(AM). Posterior endoderm and mesoderm (PEM), or posterior endoderm without its
associated mesoderm (PE), was also isolated from control and
Gsk3ß-injected embryos (PE+Gsk3ß). (B,C) Bar charts
showing the normalized relative mRNA expression levels from RT-PCR of the
liver marker for1, heart marker cardiac-troponin and the
pan-endodermal marker endodermin. WE, whole embryo; AE+AM, endoderm
and mesoderm separated and immediately recombined.